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Development of an automated DNA purification module using a micro-fabricated pillar chip
Author(s) -
Benjamin J. Hindson,
Dora M. Gutierrez,
Kevin D. Ness,
Anthony J. Makarewicz,
Thomas R. Metz,
Ujwal S. Setlur,
William B. Benett,
Jeffrey M. Loge,
Bill W. Colston,
Paul S. Francis,
Neil W. Barnett,
John M. Dzenitis
Publication year - 2007
Publication title -
the analyst
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.998
H-Index - 153
eISSN - 1364-5528
pISSN - 0003-2654
DOI - 10.1039/b713332d
Subject(s) - chromatography , chip , microfluidics , elution , volume (thermodynamics) , volumetric flow rate , fluidics , extraction (chemistry) , chemistry , chaotropic agent , dna extraction , materials science , nanotechnology , polymerase chain reaction , computer science , telecommunications , biochemistry , physics , quantum mechanics , aerospace engineering , engineering , gene
We present a fully automated DNA purification module comprised of a micro-fabricated chip and sequential injection analysis system that is designed for use within autonomous instruments that continuously monitor the environment for the presence of biological threat agents. The chip has an elliptical flow channel containing a bed (3.5 x 3.5 mm) of silica-coated pillars with height, width and center-to-center spacing of 200, 15, and 30 microm, respectively, which provides a relatively large surface area (ca. 3 cm(2)) for DNA capture in the presence of chaotropic agents. We have characterized the effect of various fluidic parameters on extraction performance, including sample input volume, capture flow rate, and elution volume. The flow-through design made the pillar chip completely reusable; carryover was eliminated by flushing lines with sodium hypochlorite and deionized water between assays. A mass balance was conducted to determine the fate of input DNA not recovered in the eluent. The device was capable of purifying and recovering Bacillus anthracis genomic DNA (input masses from 0.32 to 320 pg) from spiked environmental aerosol samples, for subsequent analysis using polymerase chain reaction-based assays.

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